B3 agonists or anticholinergics in the treatment of the lower urinary tract dysfunction in patients with multiple sclerosis?-A randomized study.


Journal

World journal of urology
ISSN: 1433-8726
Titre abrégé: World J Urol
Pays: Germany
ID NLM: 8307716

Informations de publication

Date de publication:
Aug 2021
Historique:
received: 30 10 2020
accepted: 05 12 2020
pubmed: 3 1 2021
medline: 11 1 2022
entrez: 2 1 2021
Statut: ppublish

Résumé

Multiple sclerosis (MS) is the most frequent autoimmune demyelinating disease of the central nervous system. MS patients usually present with lower urinary tract dysfunction (LUTD). Objective of this study is to evaluate and compare the efficacy and safety of treating MS patients with LUTD with either a b3 agonist (mirabegron) or anticholinergics. The study's primary outcome is the LUTD symptom improvement. This is a multi-center, single-blinded, comparative study including 91 MS patients with LUTD. At baseline, patients underwent thorough clinical examination, urine cultivation and abdominal ultrasound and completed urination diaries and specific, validated questionnaires (NBSS, MusiQoL). At second visit, patients were administered either mirabegron or anticholinergics. Treatment was always carried out alongside with MS treatment. Reevaluation was performed 3 months after first visit. Patients underwent the same clinical and imaging tests that were carried out at first visit. We compared several clinical and imaging parameters between the two groups at first visit and month 3 after treatment. Νo statistical difference was noted between the mirabegron group and the anticholinergic group in terms of LUTD improvement. In both groups, improvement from baseline regarding LUTD was recorded. Statistical analysis was performed using the paired and unpaired t test method. No patient discontinued either medication due to side effects. MS patients receiving either mirabegron or anticholinergic therapy for LUTD showed improvement. Nevertheless, no statistical difference was noted between the two cohorts at 3 months in terms of drug efficacy in all the statistically significant parameters.

Identifiants

pubmed: 33386947
doi: 10.1007/s00345-020-03555-8
pii: 10.1007/s00345-020-03555-8
doi:

Substances chimiques

Acetanilides 0
Adrenergic beta-3 Receptor Agonists 0
Cholinergic Antagonists 0
Thiazoles 0
mirabegron MVR3JL3B2V

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

3049-3056

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.

Références

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Auteurs

I Glykas (I)

Department of Urology, General Hospital of Athens G. Gennimatas, Athens, Greece. giannis.glykas@gmail.com.

Ch Fragkoulis (C)

Department of Urology, General Hospital of Athens G. Gennimatas, Athens, Greece.

D D Mitsikostas (DD)

1st Department of Neurology, Aiginiteio Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

A Papatsoris (A)

2nd Department of Urology, Sismanoglio Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

I Mitsogiannis (I)

2nd Department of Urology, Sismanoglio Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

G Papadopoulos (G)

Department of Urology, General Hospital of Athens G. Gennimatas, Athens, Greece.

A Skolarikos (A)

2nd Department of Urology, Sismanoglio Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

I Gkialas (I)

Department of Urology, General Hospital of Athens G. Gennimatas, Athens, Greece.

K Ntoumas (K)

Department of Urology, General Hospital of Athens G. Gennimatas, Athens, Greece.

A Dellis (A)

2nd Department of Surgery, Aretaieion Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
1st Department of Urology, Laiko Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

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